Cas 1155315-94-8,bis{1-[4-(2-methoxybenzyl)-6-(4-methoxyphenyl)-2H-pyridazin-3-ylidene]-2-butan-2,3-ylidene} hydrazine

1155315-94-8

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Basic information

Product Name: bis{1-[4-(2-methoxybenzyl)-6-(4-methoxyphenyl)-2H-pyridazin-3-ylidene]-2-butan-2,3-ylidene} hydrazine
Synonyms:
CAS NO:1155315-94-8
Molecular Formula:
Molecular Weight: 722.847
EINECS: N/A
Product Categories: N/A
Mol File: 1155315-94-8.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: bis{1-[4-(2-methoxybenzyl)-6-(4-methoxyphenyl)-2H-pyridazin-3-ylidene]-2-butan-2,3-ylidene} hydrazine(CAS DataBase Reference)
NIST Chemistry Reference: bis{1-[4-(2-methoxybenzyl)-6-(4-methoxyphenyl)-2H-pyridazin-3-ylidene]-2-butan-2,3-ylidene} hydrazine(1155315-94-8)
EPA Substance Registry System: bis{1-[4-(2-methoxybenzyl)-6-(4-methoxyphenyl)-2H-pyridazin-3-ylidene]-2-butan-2,3-ylidene} hydrazine(1155315-94-8)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1155315-94-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1155315-94-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,5,3,1 and 5 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1155315-94:
(9*1)+(8*1)+(7*5)+(6*5)+(5*3)+(4*1)+(3*5)+(2*9)+(1*4)=138
138 % 10 = 8
So 1155315-94-8 is a valid CAS Registry Number.

1155315-94-8Upstream product

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1155315-94-8Relevant articles and documents

Novel pyridazine derivatives: Synthesis and antimicrobial activity evaluation

Kandile,Mohamed,Zaky,Mohamed

experimental part, p. 1989 - 1996 (2009/09/08)

A general method for the preparation of new hydrazones is reported. The 1-[4-(2-methoxybenzyl)-6-aryl pyridazin-3(2H)-ylidene] hydrazines or their tautomeric structures (1a-d) were condensed with different aldehydes, dialdehydes, ketones, α-dic

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